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ABSTRACT: Background
Glioblastoma (GBM) stemlike cells (GSCs) are thought to be responsible for the maintenance and aggressiveness of GBM, the most common primary brain tumor in adults. This study aims at elucidating the involvement of deregulations within the imprinted delta-like homolog 1 gene?type III iodothyronine deiodinase gene (DLK-DIO3) region on chromosome 14q32 in GBM pathogenesis.Methods
Real-time PCR analyses were performed on GSCs and GBM tissues. Methylation analyses, gene expression, and reverse-phase protein array profiles were used to investigate the tumor suppressor function of the maternally expressed 3 gene (MEG3).Results
Loss of expression of genes and noncoding RNAs within the DLK1-DIO3 region was observed in GSCs and GBM tissues compared with normal brain. This downregulation is mainly mediated by epigenetic silencing. Kaplan-Meier analysis indicated that low expression of MEG3 and MEG8 long noncoding (lnc)RNAs significantly correlated with short survival in GBM patients. MEG3 restoration impairs tumorigenic abilities of GSCs in vitro by inhibiting cell growth, migration, and colony formation and decreases in vivo tumor growth, reducing infiltrative growth. These effects were associated with modulation of genes involved in cell adhesion and epithelial-to-mesenchymal transition (EMT).Conclusion
In GBM, MEG3 acts as a tumor suppressor mainly regulating cell adhesion, EMT, and cell proliferation, thus providing a potential candidate for novel GBM therapies.
SUBMITTER: Buccarelli M
PROVIDER: S-EPMC7746944 | biostudies-literature | 2020 Dec
REPOSITORIES: biostudies-literature
Buccarelli Mariachiara M Lulli Valentina V Giuliani Alessandro A Signore Michele M Martini Maurizio M D'Alessandris Quintino G QG Giannetti Stefano S Novelli Agnese A Ilari Ramona R Giurato Giorgio G Boe Alessandra A Castellani Giorgia G Spartano Serena S Marangi Giuseppe G Biffoni Mauro M Genuardi Maurizio M Pallini Roberto R Marziali Giovanna G Ricci-Vitiani Lucia L
Neuro-oncology 20201201 12
<h4>Background</h4>Glioblastoma (GBM) stemlike cells (GSCs) are thought to be responsible for the maintenance and aggressiveness of GBM, the most common primary brain tumor in adults. This study aims at elucidating the involvement of deregulations within the imprinted delta-like homolog 1 gene‒type III iodothyronine deiodinase gene (DLK-DIO3) region on chromosome 14q32 in GBM pathogenesis.<h4>Methods</h4>Real-time PCR analyses were performed on GSCs and GBM tissues. Methylation analyses, gene ex ...[more]